Sterilization of medical devices. Validation and routine control of sterilization by moist heatThis European Standard specifies requirements for the process development, validation, process control and monitoring of the sterilization of medical devices using moist heat. This method is based on the monitoring of the physical factors that cause the product to become sterile and presupposes that prior to validation the sterilizer and its installation conform to an appropriate specification. This European Standard does not describe a quality

additional testing may be required

but for the purposes of this standard

Neither does it apply to building documentation

Contents of BS ISO/IEC 24713-1 includes:

in straight lengths of case hardening steels

It does not cover cold rolled products and cut lengths produced from strip or sheet by cutting

which draws together a wealth of good practices for both the director and the implementing manager

for use by record management professionals and those charged with managing records in their organizations

are intended to take precedence over the corresponding general requirements

This European Standard specifies a method for the determination of the shape index of coarse aggregates

This standard specifies the requirements to be met by the manufacturer to ensure the safety of persons and property during commissioning

unless otherwise agreed at the time of inquiry and order